| Literature DB >> 30955892 |
William M Shaw1, Hitoshi Yamauchi2, Jack Mead2, Glen-Oliver F Gowers1, David J Bell3, David Öling4, Niklas Larsson4, Mark Wigglesworth5, Graham Ladds6, Tom Ellis7.
Abstract
G protein-coupled receptor (GPCR) signaling is the primary method eukaryotes use to respond to specific cues in their environment. However, the relationship between stimulus and response for each GPCR is difficult to predict due to diversity in natural signal transduction architecture and expression. Using genome engineering in yeast, we constructed an insulated, modular GPCR signal transduction system to study how the response to stimuli can be predictably tuned using synthetic tools. We delineated the contributions of a minimal set of key components via computational and experimental refactoring, identifying simple design principles for rationally tuning the dose response. Using five different GPCRs, we demonstrate how this enables cells and consortia to be engineered to respond to desired concentrations of peptides, metabolites, and hormones relevant to human health. This work enables rational tuning of cell sensing while providing a framework to guide reprogramming of GPCR-based signaling in other systems.Entities:
Keywords: G protein-coupled receptor; Saccharomyces cerevisiae; biosensor; cell signaling; cell-to-cell communication; genome engineering; synthetic biology
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Year: 2019 PMID: 30955892 PMCID: PMC6476273 DOI: 10.1016/j.cell.2019.02.023
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582